nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A convergent asymmetric synthesis of a growth hormone secretagogue
|
Zheng, Nan |
|
2003 |
14 |
22 |
p. 3435-3446 12 p. |
artikel |
2 |
A highly diastereoselective vinylogous Mannich condensation and 1,4-conjugate addition of (Z)-propenyl cuprate in the synthesis of an influenza neuraminidase inhibitor
|
Barnes, David M. |
|
2003 |
14 |
22 |
p. 3541-3551 11 p. |
artikel |
3 |
A large-scale asymmetric synthesis of (S)-cyclohexylphenyl glycolic acid
|
Su, Xiping |
|
2003 |
14 |
22 |
p. 3593-3600 8 p. |
artikel |
4 |
An alkaloid-mediated desymmetrization of meso-anhydrides via a nucleophilic ring opening with benzyl alcohol and its application in the synthesis of highly enantiomerically enriched β-amino acids
|
Bolm, Carsten |
|
2003 |
14 |
22 |
p. 3455-3467 13 p. |
artikel |
5 |
An efficient enantioselective synthesis of an indane acetic acid derivative: methyl (2S)-2-[(1S)-5-hydroxy-2,3-dihydro-1H-inden-1-yl]butanoate
|
Zhang, Mingbao |
|
2003 |
14 |
22 |
p. 3447-3453 7 p. |
artikel |
6 |
A pilot-scale synthesis of (1R)-trans-2-(2,3-dihydro-4-benzofuranyl)cyclopropanecarboxylic acid: a practical application of asymmetric cyclopropanation using a styrene as a limiting reagent
|
Simpson, James H. |
|
2003 |
14 |
22 |
p. 3569-3574 6 p. |
artikel |
7 |
A practical, two-stage preparation of benzyl (3R)-3-amino-2-oxo-1-pyrrolidinecarboxylate (2S,3S)-2,3-bis[(4-methylbenzoyl)oxy]butanediote (2:1)
|
Barrett, Roger |
|
2003 |
14 |
22 |
p. 3627-3631 5 p. |
artikel |
8 |
Assignment of the structure of a Ru(II)–BINAP catalyst
|
DiMichele, Lisa |
|
2003 |
14 |
22 |
p. 3427-3429 3 p. |
artikel |
9 |
Asymmetric synthesis on a process scale
|
|
|
2003 |
14 |
22 |
p. 3425-3426 2 p. |
artikel |
10 |
Catalytic reductive carboncarbon bond-forming reactions of alkynes
|
Miller, Karen M. |
|
2003 |
14 |
22 |
p. 3619-3625 7 p. |
artikel |
11 |
Commercialization of the hydrolytic kinetic resolution of racemic epoxides: toward the economical large-scale production of enantiopure epichlorohydrin
|
Larrow, Jay F. |
|
2003 |
14 |
22 |
p. 3589-3592 4 p. |
artikel |
12 |
Contents
|
|
|
2003 |
14 |
22 |
p. iii-iv nvt p. |
artikel |
13 |
Contributors to this issue
|
|
|
2003 |
14 |
22 |
p. v-vi nvt p. |
artikel |
14 |
Cumulative author index
|
|
|
2003 |
14 |
22 |
p. V-XX nvt p. |
artikel |
15 |
Editorial board
|
|
|
2003 |
14 |
22 |
p. IFC- 1 p. |
artikel |
16 |
Efficient synthesis of the κ-opioid receptor agonist CJ-15,161: four stereospecific inversions at a single aziridinium stereogenic center
|
Couturier, Michel |
|
2003 |
14 |
22 |
p. 3517-3523 7 p. |
artikel |
17 |
Enantiospecific and regioselective opening of 2-alkyl nosylaziridines by indoles mediated by boron trifluoride. Application to a practical synthesis of a GnRH antagonist
|
Farr, Roger N |
|
2003 |
14 |
22 |
p. 3503-3515 13 p. |
artikel |
18 |
Graphical abstracts
|
|
|
2003 |
14 |
22 |
p. vii-xiii nvt p. |
artikel |
19 |
Halide ion effects in the rhodium-catalyzed allylic substitution reaction using copper(I) alkoxides and enolates
|
Evans, P.Andrew |
|
2003 |
14 |
22 |
p. 3613-3618 6 p. |
artikel |
20 |
Instructions to contributors
|
|
|
2003 |
14 |
22 |
p. I-IV nvt p. |
artikel |
21 |
Investigation of ligand loading and asymmetric amplification in CHAOx-catalyzed asymmetric diethylzinc additions
|
Wipf, Peter |
|
2003 |
14 |
22 |
p. 3605-3611 7 p. |
artikel |
22 |
New oligomeric catalyst for the hydrolytic kinetic resolution of terminal epoxides under solvent-free conditions
|
White, David E. |
|
2003 |
14 |
22 |
p. 3633-3638 6 p. |
artikel |
23 |
New resolution approach for large-scale preparation of enantiopure didesmethylsibutramine (DDMS)
|
Han, Zhengxu |
|
2003 |
14 |
22 |
p. 3553-3556 4 p. |
artikel |
24 |
Novel enzymatic synthesis of levulinyl protected nucleosides useful for solution phase synthesis of oligonucleotides
|
Garcı́a, Javier |
|
2003 |
14 |
22 |
p. 3533-3540 8 p. |
artikel |
25 |
Practical synthesis of a cell adhesion inhibitor by self-regeneration of stereocenters
|
Yee, Nathan K. |
|
2003 |
14 |
22 |
p. 3495-3501 7 p. |
artikel |
26 |
Practical synthesis of (R)-(+)-6-(1,4-dimethoxy-3-methyl-2-naphthyl)-6-(4-hydroxyphenyl)hexanoic acid: a key intermediate for a therapeutic drug for neurodegenerative diseases
|
Ito, Tatsuya |
|
2003 |
14 |
22 |
p. 3525-3531 7 p. |
artikel |
27 |
(S)-1-Aminoindane: synthesis by chirality transfer using (R)-phenylglycine amide as chiral auxiliary
|
Uiterweerd, Patrick G.H. |
|
2003 |
14 |
22 |
p. 3479-3485 7 p. |
artikel |
28 |
Scalable, efficient process for the synthesis of (R)-3,5-bistrifluoromethylphenyl ethanol via catalytic asymmetric transfer hydrogenation and isolation as a DABCO inclusion complex
|
Hansen, Karl B. |
|
2003 |
14 |
22 |
p. 3581-3587 7 p. |
artikel |
29 |
Stereochemistry abstracts
|
|
|
2003 |
14 |
22 |
p. A645-A667 nvt p. |
artikel |
30 |
Synthesis of dirhodium(II) tetrakis[methyl 1-(3-phenylpropanoyl)-2-oxaimidazolidine-4(S)-carboxylate], Rh2(4S-MPPIM)4
|
Doyle, Michael P |
|
2003 |
14 |
22 |
p. 3601-3604 4 p. |
artikel |
31 |
The development of a practical synthesis of the potent and selective somatostatin sst3 receptor antagonist [4-(3,4-difluoro-phenyl)-piperazine-1-yl]-{(4S,4aS,8aR)-2[(S)-3-(6-methoxy-pyridin-3-yl)-2-methyl-propyl]-decahydroisoquinoline-4-yl}-methanone (NVP-ACQ090)
|
Bänziger, Markus |
|
2003 |
14 |
22 |
p. 3469-3477 9 p. |
artikel |
32 |
The preparation of enantiomerically pure cyclopropylalanine
|
Boaz, Neil W. |
|
2003 |
14 |
22 |
p. 3575-3580 6 p. |
artikel |
33 |
The synthesis of S 18986, a chiral AMPA receptor modulator, via catalytic asymmetric hydrogenation
|
Cobley, Christopher J. |
|
2003 |
14 |
22 |
p. 3431-3433 3 p. |
artikel |
34 |
Total synthesis of a second generation HIV protease inhibitor
|
Gauthier Jr., Donald R. |
|
2003 |
14 |
22 |
p. 3557-3567 11 p. |
artikel |
35 |
Total synthesis of (2R,4S,2′S,3′R)-hydroxyitraconazole: implementations of a recycle protocol and a mild and safe phase-transfer reagent for preparation of the key chiral units
|
Tanoury, Gerald J. |
|
2003 |
14 |
22 |
p. 3487-3493 7 p. |
artikel |